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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

PMFML50F — Class IIa MDD by Didactic

MD Atlas
Didactic

EUDAMED last updated this device on May 18, 2026

PMFML50F

B-03661809030918

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Didactic
UDI-DI code: 03661809030918
Reference / catalog number: PMFML50F

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Manufacturer information

Organization name: Didactic
SRN: FR-MF-000000176
Manufacturer status: Active

Related devices

PMFML80FB-03661809030956On the market PR3LVM150LFBPAFB-03661809031076On the market BPCOVSTD3661809HELE5On the market GLNP9103661809LATEVOn the market B60012IC3661809HELE5On the market

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW009
EUDAMED did not publish a description for this code.
CW001
EUDAMED did not publish a description for this code.
CW007
EUDAMED did not publish a description for this code.
CW011
It is essential to check the tightness of the connections before use

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03661809030918
Basic UDI-DI: B-03661809030918
Reference / catalog number: PMFML50F
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: Simple extension line that have a Luer Lock female, a tube and a Luer Lock fixed or mobile with a cap
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A03020101LOW PRESSURE EXTENSION LINES

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

Certificates

Certificate health across this manufacturer's portfolio.

ECM25MDR014Withdrawn
Quality management systemNotified body: 1282Expiry: Jul 28, 2030